Canonical Allele Identifier: CA1737343568
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478957G= , CM000669.2:g.117478957G= GRCh38
NC_000007.13:g.117119011G= , CM000669.1:g.117119011G= GRCh37
NC_000007.12:g.116906247G= NCBI36
NG_016465.4:g.18174G= , LRG_663:g.18174G=

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-525-287G= ENSP00000417012.1:n.-525-287G=
ENST00000673785.1:c.-406+13126G= ENSP00000501235.1:n.-406+13126G=
ENST00000546407.1:n.166+3149G=
XM_011515751.1:c.42-287G= XP_011514053.1:n.42-287G=
XM_011515752.1:c.42-287G= XP_011514054.1:n.42-287G=
XM_011515754.1:c.-1140G= XP_011514056.1:n.-1140G=